Team:HokkaidoU Japan/Notebook/Pre experiment/140910 Ptet-B0032-mRFP-dT

From 2014.igem.org

(Difference between revisions)
Line 138: Line 138:
      </ul>
      </ul>
      <div class="step-recipe">
      <div class="step-recipe">
-
P<sub>tet</sub>-B0034-mRFP-dT(6A1) SpeI_PstI_F& P<sub>tet</sub>_SpeI_R(vector), XbaI_B0032_mRFP_F& PstI_SpeI_R(insert), KOD Fx Neo
+
R0040-B0034-E1010-B0015(on pSB6A1) SpeI_PstI_F Tm:72.8&#8451;& Ptet_SpeI_R Tm:72.6&#8451; (vector)
 +
        XbaI_B0032_mRFP_F Tm:76.3&#8451; & PstI_SpeI_R Tm:74.6&#8451; (insert)
 +
        KOD Fx Neo
</div>
</div>
    </div>
    </div>
Line 159: Line 161:
      </ul>
      </ul>
      <div class="step-recipe">
      <div class="step-recipe">
-
digested PCR productions
+
PCR products
</div>
</div>
    </div>
    </div>
Line 180: Line 182:
      </ul>
      </ul>
      <div class="step-recipe">
      <div class="step-recipe">
-
Cut  vector with SpeI, PstI (using 10&times;H buffer) Cut  insert with XbaI, PstI (using 10&times;M buffer)
+
Cut  vector with SpeI, PstI (using 10&times;H buffer)  
 +
        Cut  insert with XbaI, PstI (using 10&times;M buffer)
 +
 
</div>
</div>
    </div>
    </div>
Line 188: Line 192:
  <div class="step-tile">
  <div class="step-tile">
  <h2 class="step-title">
  <h2 class="step-title">
-
Dephophorylation
+
Dephosphorylation
</h2>
</h2>
  </div>
  </div>
Line 202: Line 206:
      <div class="step-recipe">
      <div class="step-recipe">
Antactic phosphorylate insert (using 10&times;Antarctic phosphatase buffer) 37&#8451; 35min 65&#8451; 10min
Antactic phosphorylate insert (using 10&times;Antarctic phosphatase buffer) 37&#8451; 35min 65&#8451; 10min
 +
</div>
</div>
    </div>
    </div>
Line 243: Line 248:
      </ul>
      </ul>
      <div class="step-recipe">
      <div class="step-recipe">
-
ligation products on ice  30min each of 5.0&micro;L DNA to DH5&alpha;  42&#8451;        1min on ice 2min
+
R0040-B0032-E1010-B0015(on pSB1A6)
 +
        5.0&micro;L DNA to DH5&alpha;   
 +
 
</div>
</div>
    </div>
    </div>
Line 264: Line 271:
      </ul>
      </ul>
      <div class="step-recipe">
      <div class="step-recipe">
-
P<sub>tet</sub>-B0034-mRFP-dT on pSB6A1 EcoI_XbaI_F Tm:70.9&#8451; rbs_SpeI_R Tm:59.2&#8451;
+
R0040-B0032-E1010-B0015(on pSB6A1) EcoI_XbaI_F Tm:70.9&#8451; & RBS_SpeI_R Tm:59.2&#8451;
 +
 
</div>
</div>
    </div>
    </div>
Line 285: Line 293:
      </ul>
      </ul>
      <div class="step-recipe">
      <div class="step-recipe">
-
P<sub>tet</sub>-B0034-mRFP-dT on pSB6A1
+
R0040-B0032-E1010-B0015(on pSB6A1)
</div>
</div>
    </div>
    </div>
Line 293: Line 301:
  <div class="step-tile">
  <div class="step-tile">
  <h2 class="step-title">
  <h2 class="step-title">
-
mini-Prep
+
Mini-Prep
</h2>
</h2>
  </div>
  </div>
Line 306: Line 314:
      </ul>
      </ul>
      <div class="step-recipe">
      <div class="step-recipe">
-
P<sub>tet</sub>-B0034-mRFP-dT on pSB6A1
+
R0040-B0032-E1010-B0015(on pSB6A1)
</div>
</div>
    </div>
    </div>

Revision as of 00:57, 18 October 2014

Notebook
Lab Documents

Ptet-B0032-mRFP-dT

  • Start

  • PCR

    R0040-B0034-E1010-B0015(on pSB6A1) SpeI_PstI_F Tm:72.8℃& Ptet_SpeI_R Tm:72.6℃ (vector) XbaI_B0032_mRFP_F Tm:76.3℃ & PstI_SpeI_R Tm:74.6℃ (insert) KOD Fx Neo
  • Gel extraction

    PCR products
  • Digestion

    Cut vector with SpeI, PstI (using 10×H buffer) Cut insert with XbaI, PstI (using 10×M buffer)
  • Dephosphorylation

    Antactic phosphorylate insert (using 10×Antarctic phosphatase buffer) 37℃ 35min 65℃ 10min
  • Ligation

    Ligate vector with insert
  • Transformation

    R0040-B0032-E1010-B0015(on pSB1A6) 5.0µL DNA to DH5α
  • Colony PCR

    R0040-B0032-E1010-B0015(on pSB6A1) EcoI_XbaI_F Tm:70.9℃ & RBS_SpeI_R Tm:59.2℃
  • Culture

    R0040-B0032-E1010-B0015(on pSB6A1)
  • Mini-Prep

    R0040-B0032-E1010-B0015(on pSB6A1)
  • Complete!